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CAS 850567-37-2

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[3-(thiomorpholine-4-carbonyl)phenyl]boronic acid

Description:
[3-(Thiomorpholine-4-carbonyl)phenyl]boronic acid is an organic compound characterized by the presence of a boronic acid functional group, which is known for its ability to form reversible covalent bonds with diols, making it useful in various applications, including organic synthesis and medicinal chemistry. The compound features a phenyl ring substituted with a thiomorpholine-4-carbonyl group, which contributes to its unique chemical properties and potential biological activity. The thiomorpholine moiety introduces a heterocyclic structure that may enhance the compound's solubility and reactivity. As a boronic acid, it can participate in Suzuki coupling reactions, a key method for forming carbon-carbon bonds in organic synthesis. Additionally, the compound's ability to interact with biological targets makes it of interest in drug discovery and development. Its specific characteristics, such as solubility, stability, and reactivity, can vary based on environmental conditions and the presence of other functional groups. Overall, [3-(thiomorpholine-4-carbonyl)phenyl]boronic acid represents a versatile building block in both synthetic and medicinal chemistry.
Formula:C11H14BNO3S
InChI:InChI=1/C11H14BNO3S/c14-11(13-4-6-17-7-5-13)9-2-1-3-10(8-9)12(15)16/h1-3,8,15-16H,4-7H2
SMILES:c1cc(cc(c1)B(O)O)C(=O)N1CCSCC1
Synonyms:
  • [3-(Thiomorpholin-4-ylcarbonyl)phenyl]boronic acid
  • boronic acid, B-[3-(4-thiomorpholinylcarbonyl)phenyl]-
  • (3-(Thiomorpholine-4-carbonyl)phenyl)boronicacid
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